525 related articles for article (PubMed ID: 11587068)
1. Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome.
Chávez B; Méndez JP; Ulloa-Aguirre A; Larrea F; Vilchis F
J Hum Genet; 2001; 46(10):560-5. PubMed ID: 11587068
[TBL] [Abstract][Full Text] [Related]
2. Novel androgen receptor gene mutations in Australian patients with complete androgen insensitivity syndrome.
MacLean HE; Ball EM; Rekaris G; Warne GL; Zajac JD
Hum Mutat; 2004 Mar; 23(3):287. PubMed ID: 14974091
[TBL] [Abstract][Full Text] [Related]
3. Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome.
Deeb A; Mason C; Lee YS; Hughes IA
Clin Endocrinol (Oxf); 2005 Jul; 63(1):56-62. PubMed ID: 15963062
[TBL] [Abstract][Full Text] [Related]
4. Identification of a critical novel mutation in the exon 1 of androgen receptor gene in 2 brothers with complete androgen insensitivity syndrome.
Radpour R; Falah M; Aslani A; Zhong XY; Saleki A
J Androl; 2009; 30(3):230-2. PubMed ID: 19023143
[TBL] [Abstract][Full Text] [Related]
5. Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain.
Murono K; Mendonca BB; Arnhold IJ; Rigon AC; Migeon CJ; Brown TR
Hum Mutat; 1995; 6(2):152-62. PubMed ID: 7581399
[TBL] [Abstract][Full Text] [Related]
6. [An acceptor-splice-site mutation responsible for complete androgen insensitivity syndrome].
Zhang W; Li X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):14-6. PubMed ID: 11172634
[TBL] [Abstract][Full Text] [Related]
7. Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome.
Raicu F; Giuliani R; Gatta V; Palka C; Franchi PG; Lelli-Chiesa P; Tumini S; Stuppia L
Asian J Androl; 2008 Jul; 10(4):687-91. PubMed ID: 18097502
[TBL] [Abstract][Full Text] [Related]
8. [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome].
Soriano Guillén L; Muñoz Calvo MT; Martinez Pérez J; Pozo Román J; Martín Sobrino MA; González Medeiro I; Argente Oliver J
An Esp Pediatr; 2002 Apr; 56(4):347-52. PubMed ID: 11927080
[TBL] [Abstract][Full Text] [Related]
9. Altered mRNA expression due to insertion or substitution of thymine at position +3 of two splice-donor sites in the androgen receptor gene.
Trifiro MA; Lumbroso R; Beitel LK; Vasiliou DM; Bouchard J; Deal C; Van Vliet G; Pinsky L
Eur J Hum Genet; 1997; 5(1):50-8. PubMed ID: 9156321
[TBL] [Abstract][Full Text] [Related]
10. Five novel androgen receptor gene mutations associated with complete androgen insensitivity syndrome.
Jääskeläinen J; Mongan NP; Harland S; Hughes IA
Hum Mutat; 2006 Mar; 27(3):291. PubMed ID: 16470553
[TBL] [Abstract][Full Text] [Related]
11. Novel point mutation in the splice donor site of exon-intron junction 6 of the androgen receptor gene in a patient with partial androgen insensitivity syndrome.
Sammarco I; Grimaldi P; Rossi P; Cappa M; Moretti C; Frajese G; Geremia R
J Clin Endocrinol Metab; 2000 Sep; 85(9):3256-61. PubMed ID: 10999818
[TBL] [Abstract][Full Text] [Related]
12. Comparison of the molecular consequences of different mutations at residue 754 and 690 of the androgen receptor (AR) and androgen insensitivity syndrome (AIS) phenotype.
Tadokoro R; Bunch T; Schwabe JW; Hughes IA; Murphy JC
Clin Endocrinol (Oxf); 2009 Aug; 71(2):253-60. PubMed ID: 19178528
[TBL] [Abstract][Full Text] [Related]
13. Analysis of exon 1 mutations in the androgen receptor gene.
Gottlieb B; Vasiliou DM; Lumbroso R; Beitel LK; Pinsky L; Trifiro MA
Hum Mutat; 1999; 14(6):527-39. PubMed ID: 10571951
[TBL] [Abstract][Full Text] [Related]
14. Complete androgen insensitivity without Wolffian duct development: the AR-A form of the androgen receptor is not sufficient for male genital development.
Barbaro M; Oscarson M; Almskog I; Hamberg H; Wedell A
Clin Endocrinol (Oxf); 2007 Jun; 66(6):822-6. PubMed ID: 17408421
[TBL] [Abstract][Full Text] [Related]
15. Novel and recurrent mutations in patients with androgen insensitivity syndromes.
Ledig S; Jakubiczka S; Neulen J; Aulepp U; Burck-Lehmann U; Mohnike K; Thiele H; Zierler H; Brewer C; Wieacker P
Horm Res; 2005; 63(6):263-9. PubMed ID: 15925895
[TBL] [Abstract][Full Text] [Related]
16. The clinical and molecular spectrum of androgen insensitivity syndromes.
Hiort O; Sinnecker GH; Holterhus PM; Nitsche EM; Kruse K
Am J Med Genet; 1996 May; 63(1):218-22. PubMed ID: 8723113
[TBL] [Abstract][Full Text] [Related]
17. Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one case.
Yen JL; Chang KH; Sheu JC; Lee YJ; Tsai LP
Acta Paediatr Taiwan; 2005; 46(2):101-5. PubMed ID: 16302589
[TBL] [Abstract][Full Text] [Related]
18. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
19. A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndrome.
Dörk T; Schnieders F; Jakubiczka S; Wieacker P; Schroeder-Kurth T; Schmidtke J
Hum Mutat; 1998; 11(4):337-9. PubMed ID: 9554754
[TBL] [Abstract][Full Text] [Related]
20. Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred.
Belsham DD; Pereira F; Greenberg CR; Liao S; Wrogemann K
Hum Mutat; 1995; 5(1):28-33. PubMed ID: 7537149
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
